A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695339



Internal ID15431991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98570021..98589420hg38UCSC Ensembl
Innerchr15:99113250..99132649hg19UCSC Ensembl
Innerchr15:96930773..96950172hg18UCSC Ensembl
Innerchr15:96930773..96950172hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3819400
hg1919400
hg1819400
hg1719400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517927
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695339
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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